A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770409



Internal ID18966854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74782058..74782559hg38UCSC Ensembl
chr15:75074399..75074900hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069866
Supporting Variants
SamplesKWP1
Known GenesCSK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770409
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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